Literature DB >> 18623202

Congenital Ewing sarcoma in retroperitoneum with multiple metastases.

Yusuke Saito1, Akinobu Matsuzaki, Aiko Suminoe, Yuhki Koga, Hiroaki Kurata, Yoshinao Oda, Masazumi Tsuneyoshi, Toshiro Hara.   

Abstract

A 7-day-old Japanese female showed the absence of spontaneous movement in her both legs. MRI revealed tumors in the retroperitoneum invading into the spinal canal, the left cerebral hemisphere and the right eyeball. Histological examination of retroperitoneal tumor revealed the sheets of undifferentiated small round cells with hyperchromatic nuclei and scanty cytoplasm. EWS-FLI1 fusion gene was detected by RT-PCR, indicating Ewing sarcoma. She received chemo-radiotherapy and survived for 2 years and 10 months despite the multiple metastases at initial presentation. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18623202     DOI: 10.1002/pbc.21678

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

1.  Chondrosarcoma Metastasis to the Choroid.

Authors:  Jenna May Kim; Amanda J Wong; Amanda J Lu; Renelle Pointdujour-Lim
Journal:  Ocul Oncol Pathol       Date:  2019-01-17

2.  Congenital soft tissue Ewing's sarcoma: A case report of pre- and postnatal magnetic resonance imaging findings.

Authors:  Chaoxiang Yang; Wenjun Chen; Penghui Han
Journal:  Medicine (Baltimore)       Date:  2022-01-14       Impact factor: 1.817

  2 in total

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